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Cell Therapeutics, Inc. (CTI) Plans to Submit Supplemental Biologics License Application (sBLA) for ZEVALIN(R) Consolidation of First Remission in Advanced Stage Follicular Lymphoma in 2008
Date:11/27/2007

ional Randomized Phase

3 First-Line Indolent Trial (FIT) in

414 Patients.

Monday, 5:00 #631-III Radioimmunotherapy with 90Y-

Dec. 10, PM (3412) Ibritumomab Tiuxetan (Zevalin)

2007 as Consolidation of First Remission

in Patients with Advanced Stage

Follicular Lymphoma: A Real-Time MBR

RQ-PCR Analysis.

Monday, 5:00 #664-III CHOP-R (Cyclophosphamide,

Dec. 10, PM (3445) Doxorubicin, Vincristine, Prednisone,

2007 Rituximab) Compared to CPOP-R

(Cyclophosphamide, Pixantrone,

Vincristine, Prednisone, Rituxamib)

in First-Line Therapy of Diffuse

Large B Cell Lymphoma (DLBCL): An

Interim Analysis.

For more information about the ASH annual meeting and for a complete list of abstracts, please refer to the conference Web site at http://www.hematology.org.

About ZEVALIN(R)

ZEVALIN(R) (Ibritumomab Tiuxetan) is a form of cancer therapy called radioimmunotherapy and is indicated for the treatment of patients with relapsed or refractory low-grade or follicular B-cell NHL, including patients with Rituximab-refractory NHL. It was approved by the FDA in February of 2002 as the first radioimmunotherapeutic agent for the treatment of NHL.

Deaths associated with an infusion reaction symptom complex have occurred within 24 hours of rituximab infusions. Yttrium-90 ZEVALIN administration results in severe and prolonged cytopenia
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SOURCE Cell Therapeutics, Inc.
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